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◆ Chemical communications (Cambridge, England)2026-09-22

Ring-opening radical recombination strategy based on benzothiazolium salts: synthesis of 1,4-benzothiazin-3-one derivatives.

Jiaxin Liang, Zhixin Lai, Yaqi Zhan, Zheng Zeng, Zipeng Zeng, Zhongzhi Zhu, Xiuwen Chen

原始摘要(英文原文)· Original abstract
This work describes a ferrocene- and oxygen-mediated ring-opening radical recombination of benzothiazolium salts, enabling a three-component tandem reaction with anilines and benzaldehydes to rapidly build the 1,4-benzothiazin-3-one skeleton through C-S bond cleavage and sequential formation of C-O, C-N and C-S bonds.
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Ring-opening radical recombination strategy based on benzothiazolium salts: synthesis of 1,4-benzothiazin-3-one derivatives. — 科研速览 Science Skim